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局部超氧化物歧化酶活性和脂质过氧化物水平在镉神经毒性中的可能作用:对生长中大鼠的体内和体外研究

Possible role of regional superoxide dismutase activity and lipid peroxide levels in cadmium neurotoxicity: in vivo and in vitro studies in growing rats.

作者信息

Shukla G S, Hussain T, Chandra S V

机构信息

Industrial Toxicology Research Centre, Lucknow, India.

出版信息

Life Sci. 1987 Nov 9;41(19):2215-21. doi: 10.1016/0024-3205(87)90518-2.

DOI:10.1016/0024-3205(87)90518-2
PMID:3669920
Abstract

Cd2+ (0.4 mg/kg) administration to growing rats (45 +/- 5 g) intraperitoneally, daily for 30 days was found to decrease the activity of superoxide dismutase (SOD) in all the brain regions, except hippocampus. The concentrations of lipid peroxides were significantly elevated in the cerebellum, cerebral cortex, corpus striatum and midbrain. A 100% inhibition in SOD activity was observed by 14 microM and 50 microM of Cd2+ in bovine blood and rat brain preparations, respectively. Cadmium-induced strong inhibitory effect on brain and purified bovine blood SOD suggested a direct effect of the metal on enzyme molecule. Furthermore, in vitro addition of a wide range of Cd2+ (1-100 microM) increased the rate of lipid peroxidation (LPO) reaction in fresh brain homogenate, however, did not affect boiled homogenate. The studies on LPO in reconstituted homogenate resulting from mixing of fresh and/or heated different subcellular fractions indicated the presence of some heat-labile Cd2+ -sensitive factor in 15000 x g pellet fraction. It is suggested that Cd2+ directly and indirectly through inhibition of SOD, increases the LPO of cell membranes and thus produces damage to the associated physiological functions leading to central nervous dysfunctions.

摘要

对体重为45±5克的生长中大鼠腹腔内每日注射Cd2+(0.4毫克/千克),持续30天,结果发现除海马体外,所有脑区的超氧化物歧化酶(SOD)活性均降低。小脑、大脑皮层、纹状体和中脑的脂质过氧化物浓度显著升高。在牛血和大鼠脑匀浆制剂中,分别在14微摩尔和50微摩尔的Cd2+浓度下观察到SOD活性受到100%抑制。镉对脑和纯化牛血SOD产生的强烈抑制作用表明该金属对酶分子有直接影响。此外,体外添加一系列浓度的Cd2+(1 - 100微摩尔)可提高新鲜脑匀浆中脂质过氧化(LPO)反应的速率,但对煮沸的匀浆无影响。对由新鲜和/或加热的不同亚细胞组分混合而成的重组匀浆中LPO的研究表明,在15000×g沉淀组分中存在一些对热不稳定的Cd2+敏感因子。提示Cd2+通过抑制SOD直接或间接增加细胞膜的LPO,从而对相关生理功能造成损害,导致中枢神经功能障碍。

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